Nartop Dilek, Hasanoğlu Özkan Elvan, Öğütcü Hatice, Kurnaz Yetim Nurdan, Özdemir İnci
Department of Chemistry, Faculty of Arts and Sciences, Düzce University Düzce Turkiye.
Department of Chemistry, Faculty of Sciences, Gazi University Ankara Turkiye
RSC Adv. 2024 Sep 16;14(40):29308-29318. doi: 10.1039/d4ra04002c. eCollection 2024 Sep 12.
In this paper, eight novel α-N-heterocyclic thiosemicarbazone complexes were synthesized in search of new biologically active compounds, and characterized organic elemental analysis, nuclear magnetic resonance spectroscopy, infrared spectra, thermogravimetric analysis, ultraviolet-visible spectroscopy, molar conductance and magnetic susceptibility measurements. The antimicrobial activity of these complexes was examined against ten disease-causing pathogens: Gram-positive bacteria ( ATCC9341, ATCC12228, RSKK863) and Gram-negative bacteria ( ATCC27853, ATCC27853, ATCC51342, H NCTC9018394, NCTC2966, RSKK96026) and yeast ( Y-1200-NIH). The results revealed that the α-N-heterocyclic thiosemicarbazone compounds showed potent activity. It was observed that all thiosemicarbazone complexes were more susceptible to Gram-negative strains based on the presence of an electron-withdrawing substituent (-Br/-Cl/-F). It was determined that thiosemicarbazone Cucomplexes showed stronger antifungal effects.
本文合成了八种新型α-N-杂环硫代卡巴腙配合物以寻找新的生物活性化合物,并通过有机元素分析、核磁共振光谱、红外光谱、热重分析、紫外可见光谱、摩尔电导率和磁化率测量对其进行了表征。考察了这些配合物对十种致病病原体的抗菌活性:革兰氏阳性菌(ATCC9341、ATCC12228、RSKK863)和革兰氏阴性菌(ATCC27853、ATCC27853、ATCC51342、H NCTC9018394、NCTC2966、RSKK96026)以及酵母(Y-1200-NIH)。结果表明,α-N-杂环硫代卡巴腙化合物显示出强效活性。基于吸电子取代基(-Br/-Cl/-F)的存在,观察到所有硫代卡巴腙配合物对革兰氏阴性菌株更敏感。确定硫代卡巴腙铜配合物显示出更强效的抗真菌作用。